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Epileptic high-frequency network activity in a model of non-lesional temporal lobe epilepsy
High-frequency cortical activity, particularly in the 250–600 Hz (fast ripple) band, has been implicated in playing a crucial role in epileptogenesis and seizure generation. Fast ripples are highly specific for the seizure initiation zone. However, evidence for the association of fast ripples with e...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2859153/ https://www.ncbi.nlm.nih.gov/pubmed/20400525 http://dx.doi.org/10.1093/brain/awq070 |
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author | Jiruska, Premysl Finnerty, Gerald T. Powell, Andrew D. Lofti, Noosheen Cmejla, Roman Jefferys, John G. R. |
author_facet | Jiruska, Premysl Finnerty, Gerald T. Powell, Andrew D. Lofti, Noosheen Cmejla, Roman Jefferys, John G. R. |
author_sort | Jiruska, Premysl |
collection | PubMed |
description | High-frequency cortical activity, particularly in the 250–600 Hz (fast ripple) band, has been implicated in playing a crucial role in epileptogenesis and seizure generation. Fast ripples are highly specific for the seizure initiation zone. However, evidence for the association of fast ripples with epileptic foci depends on animal models and human cases with substantial lesions in the form of hippocampal sclerosis, which suggests that neuronal loss may be required for fast ripples. In the present work, we tested whether cell loss is a necessary prerequisite for the generation of fast ripples, using a non-lesional model of temporal lobe epilepsy that lacks hippocampal sclerosis. The model is induced by unilateral intrahippocampal injection of tetanus toxin. Recordings from the hippocampi of freely-moving epileptic rats revealed high-frequency activity (>100 Hz), including fast ripples. High-frequency activity was present both during interictal discharges and seizure onset. Interictal fast ripples proved a significantly more reliable marker of the primary epileptogenic zone than the presence of either interictal discharges or ripples (100–250 Hz). These results suggest that fast ripple activity should be considered for its potential value in the pre-surgical workup of non-lesional temporal lobe epilepsy. |
format | Text |
id | pubmed-2859153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28591532010-04-26 Epileptic high-frequency network activity in a model of non-lesional temporal lobe epilepsy Jiruska, Premysl Finnerty, Gerald T. Powell, Andrew D. Lofti, Noosheen Cmejla, Roman Jefferys, John G. R. Brain Original Articles High-frequency cortical activity, particularly in the 250–600 Hz (fast ripple) band, has been implicated in playing a crucial role in epileptogenesis and seizure generation. Fast ripples are highly specific for the seizure initiation zone. However, evidence for the association of fast ripples with epileptic foci depends on animal models and human cases with substantial lesions in the form of hippocampal sclerosis, which suggests that neuronal loss may be required for fast ripples. In the present work, we tested whether cell loss is a necessary prerequisite for the generation of fast ripples, using a non-lesional model of temporal lobe epilepsy that lacks hippocampal sclerosis. The model is induced by unilateral intrahippocampal injection of tetanus toxin. Recordings from the hippocampi of freely-moving epileptic rats revealed high-frequency activity (>100 Hz), including fast ripples. High-frequency activity was present both during interictal discharges and seizure onset. Interictal fast ripples proved a significantly more reliable marker of the primary epileptogenic zone than the presence of either interictal discharges or ripples (100–250 Hz). These results suggest that fast ripple activity should be considered for its potential value in the pre-surgical workup of non-lesional temporal lobe epilepsy. Oxford University Press 2010-05 2010-04-16 /pmc/articles/PMC2859153/ /pubmed/20400525 http://dx.doi.org/10.1093/brain/awq070 Text en © The Author(s) 2010. Published by Oxford University Press on behalf of Brain. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Jiruska, Premysl Finnerty, Gerald T. Powell, Andrew D. Lofti, Noosheen Cmejla, Roman Jefferys, John G. R. Epileptic high-frequency network activity in a model of non-lesional temporal lobe epilepsy |
title | Epileptic high-frequency network activity in a model of non-lesional temporal lobe epilepsy |
title_full | Epileptic high-frequency network activity in a model of non-lesional temporal lobe epilepsy |
title_fullStr | Epileptic high-frequency network activity in a model of non-lesional temporal lobe epilepsy |
title_full_unstemmed | Epileptic high-frequency network activity in a model of non-lesional temporal lobe epilepsy |
title_short | Epileptic high-frequency network activity in a model of non-lesional temporal lobe epilepsy |
title_sort | epileptic high-frequency network activity in a model of non-lesional temporal lobe epilepsy |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2859153/ https://www.ncbi.nlm.nih.gov/pubmed/20400525 http://dx.doi.org/10.1093/brain/awq070 |
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